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Evaluation of a new, rapid, simple test for the detection of influenza virus
BACKGROUND: Influenza virus infections are responsible for significant morbidity and mortality in both pediatric and adult populations worldwide. Rapid and accurate diagnosis of influenza is necessary for appropriate patient management during the influenza season and for optimal utilization of anti-...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4369360/ https://www.ncbi.nlm.nih.gov/pubmed/25656393 http://dx.doi.org/10.1186/s12879-015-0775-5 |
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author | Hurtado, Juan Carlos Mosquera, Maria Mar de Lazzari, Elisa Martínez, Esteban Torner, Nuria Isanta, Ricard de Molina, Patricia Pumarola, Tomás Marcos, Maria Angeles Estape, Jordi Vila |
author_facet | Hurtado, Juan Carlos Mosquera, Maria Mar de Lazzari, Elisa Martínez, Esteban Torner, Nuria Isanta, Ricard de Molina, Patricia Pumarola, Tomás Marcos, Maria Angeles Estape, Jordi Vila |
author_sort | Hurtado, Juan Carlos |
collection | PubMed |
description | BACKGROUND: Influenza virus infections are responsible for significant morbidity and mortality in both pediatric and adult populations worldwide. Rapid and accurate diagnosis of influenza is necessary for appropriate patient management during the influenza season and for optimal utilization of anti-influenza therapy. We prospectively tested the accuracy of a simple and rapid diagnostic method. METHODS: Ninety-eight samples (nasal and pharyngeal swabs) from patients with upper respiratory tract infection symptoms who presented to primary healthcare centres in Barcelona (Spain) were prospectively analyzed. The samples were collected as part of influenza surveillance program. Samples that had enough volume to make the new test after aliquoting the amount needed to perform routine tests were included. None of the samples were pre-selected as a result of their status in relation to influenza virus. Samples were analyzed by in-house real-time PCR and Alere™ i Influenza A & B (Alere™ i), which uses isothermal amplification of nucleic acids for the qualitative detection of influenza A and B in nasal swabs transported in viral transport media. The two techniques were compared by positive percent agreement (PPA) and negative percent agreement (NPA). Statistical analysis was performed with Stata. RESULTS: Of the 98 samples analysed 90 were concordant; 46 (46.9%) were positive and 44 (44.9%) were negative. Five samples showed invalid results with the Alere™ i test and could be not re-tested due to insufficient sample volume and were not included in the final statistical analysis. In the 93 remaining samples, the Alere™ i test showed 97% of accuracy having correctly classified 90 samples. We obtained discordant results in 3 samples (3%). The PPA was 93.8% for influenza A and 94.1% for influenza B, and NPA was 100% for influenza A and influenza B virus. In addition, the Alere™ i was very rapid (15 minutes or less) and extremely easy to use. CONCLUSIONS: The Alere™ i test provided a good correlation compared to the real-time PCR test for the diagnosis of influenza. Since this method can be performed in minutes, it allows immediate, accurate clinical decisions to prescribe appropriate antiviral treatment or isolation of patients. |
format | Online Article Text |
id | pubmed-4369360 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-43693602015-03-23 Evaluation of a new, rapid, simple test for the detection of influenza virus Hurtado, Juan Carlos Mosquera, Maria Mar de Lazzari, Elisa Martínez, Esteban Torner, Nuria Isanta, Ricard de Molina, Patricia Pumarola, Tomás Marcos, Maria Angeles Estape, Jordi Vila BMC Infect Dis Research Article BACKGROUND: Influenza virus infections are responsible for significant morbidity and mortality in both pediatric and adult populations worldwide. Rapid and accurate diagnosis of influenza is necessary for appropriate patient management during the influenza season and for optimal utilization of anti-influenza therapy. We prospectively tested the accuracy of a simple and rapid diagnostic method. METHODS: Ninety-eight samples (nasal and pharyngeal swabs) from patients with upper respiratory tract infection symptoms who presented to primary healthcare centres in Barcelona (Spain) were prospectively analyzed. The samples were collected as part of influenza surveillance program. Samples that had enough volume to make the new test after aliquoting the amount needed to perform routine tests were included. None of the samples were pre-selected as a result of their status in relation to influenza virus. Samples were analyzed by in-house real-time PCR and Alere™ i Influenza A & B (Alere™ i), which uses isothermal amplification of nucleic acids for the qualitative detection of influenza A and B in nasal swabs transported in viral transport media. The two techniques were compared by positive percent agreement (PPA) and negative percent agreement (NPA). Statistical analysis was performed with Stata. RESULTS: Of the 98 samples analysed 90 were concordant; 46 (46.9%) were positive and 44 (44.9%) were negative. Five samples showed invalid results with the Alere™ i test and could be not re-tested due to insufficient sample volume and were not included in the final statistical analysis. In the 93 remaining samples, the Alere™ i test showed 97% of accuracy having correctly classified 90 samples. We obtained discordant results in 3 samples (3%). The PPA was 93.8% for influenza A and 94.1% for influenza B, and NPA was 100% for influenza A and influenza B virus. In addition, the Alere™ i was very rapid (15 minutes or less) and extremely easy to use. CONCLUSIONS: The Alere™ i test provided a good correlation compared to the real-time PCR test for the diagnosis of influenza. Since this method can be performed in minutes, it allows immediate, accurate clinical decisions to prescribe appropriate antiviral treatment or isolation of patients. BioMed Central 2015-02-06 /pmc/articles/PMC4369360/ /pubmed/25656393 http://dx.doi.org/10.1186/s12879-015-0775-5 Text en © Hurtado et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Hurtado, Juan Carlos Mosquera, Maria Mar de Lazzari, Elisa Martínez, Esteban Torner, Nuria Isanta, Ricard de Molina, Patricia Pumarola, Tomás Marcos, Maria Angeles Estape, Jordi Vila Evaluation of a new, rapid, simple test for the detection of influenza virus |
title | Evaluation of a new, rapid, simple test for the detection of influenza virus |
title_full | Evaluation of a new, rapid, simple test for the detection of influenza virus |
title_fullStr | Evaluation of a new, rapid, simple test for the detection of influenza virus |
title_full_unstemmed | Evaluation of a new, rapid, simple test for the detection of influenza virus |
title_short | Evaluation of a new, rapid, simple test for the detection of influenza virus |
title_sort | evaluation of a new, rapid, simple test for the detection of influenza virus |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4369360/ https://www.ncbi.nlm.nih.gov/pubmed/25656393 http://dx.doi.org/10.1186/s12879-015-0775-5 |
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